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HARVARD Citation
Perna, A. et al. (2018). Severe 5, 10‐methylenetetrahydrofolate reductase deficiency: a rare, treatable cause of complicated hereditary spastic paraplegia. European journal of neurology. pp. 602-605. [Online].
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Perna, A. et al. (2018). Severe 5, 10‐methylenetetrahydrofolate reductase deficiency: a rare, treatable cause of complicated hereditary spastic paraplegia. European journal of neurology. pp. 602-605. [Online].